34-24-18. Phenylketonuria, hypothyroidism, and galactosemia testing in newborn.
44 words·~1 min read·
/sd/title-34/chapter-34-24/34-24-18A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
The tests for detecting a metabolic, inherited, or genetic disorder of the newborn infant, as prescribed by the Department of Health, shall include the testing for excessive phenylalanine in the serum of the newborn, for hypothyroidism, and for elevated blood galactose in the newborn.